rs746419489
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs746419489(A;A) |
Make rs746419489(A;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 97584820 |
Gene | HOGA1 |
is a | snp |
is | mentioned by |
dbSNP | rs746419489 |
dbSNP (classic) | rs746419489 |
ClinGen | rs746419489 |
ebi | rs746419489 |
HLI | rs746419489 |
Exac | rs746419489 |
Gnomad | rs746419489 |
Varsome | rs746419489 |
LitVar | rs746419489 |
Map | rs746419489 |
PheGenI | rs746419489 |
Biobank | rs746419489 |
1000 genomes | rs746419489 |
hgdp | rs746419489 |
ensembl | rs746419489 |
geneview | rs746419489 |
scholar | rs746419489 |
rs746419489 | |
pharmgkb | rs746419489 |
gwascentral | rs746419489 |
openSNP | rs746419489 |
23andMe | rs746419489 |
SNPshot | rs746419489 |
SNPdbe | rs746419489 |
MSV3d | rs746419489 |
GWAS Ctlg | rs746419489 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs746419489(A;A) |
Alt | rs746419489(A;A) |
Reference | Rs746419489(C;C) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | HOGA1 |
CLNDBN | Primary hyperoxaluria, type III |
Reversed | 0 |
HGVS | NC_000010.10:g.99344577C>A |
CLNSRC | |
CLNACC | RCV000186475.1, |